Medical Science Liaison (MSL) -Maternal-Fetal Immunology - PST/MST

Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize resources + improve impact for all our clients. Through strategic partnerships + deep therapeutic expertise, Amplity transforms how breakthrough treatments reach the people who need them.

Medical Science Liaison (MSL) -Maternal-Fetal Immunology

US

Use your MSL/CTL, experience in an exciting new role. As an Amplity employee representing one of our top clients, a competitive base salary, bonus potential, auto allowance, full benefit package including medical, dental, vision, 401K, company funded long-term, short-term, disability, life insurance, mental wellness program, generous PTO, paid holidays and more. If you have experience in the OBYGN, maternal health field and MSL/CTL experience we would like to hear from you. US based.

Employees can expect to be paid a salary of approximately $205K - $220K. The salary range displayed may vary based on market data/ranges, an applicant's skills, prior relevant experience, certain degrees, certifications, and other relevant factors.

Summary

The MFI Medical Science Liaison (MSL) has a specialized focus that complements Medical Science Liaison (MSL)/ Clinical Trial Liaison (CTL) responsibilities. The key aspects and objectives of this role are:

• Support and enhance the enrollment of ongoing clinical studies, specifically in rare maternal-fetal diseases.
• The primary focus is on increasing recruitment into ongoing Phase 3 trials.
• Relationship Building: Establish and maintain strong relationships with healthcare professionals (HCPs) and key opinion leaders (KOLs) in the Maternal-Fetal Immunology space.
• Identify and build relationships with KOLs in adjacent specialties, including neonatology, pediatric hematology, and transfusion medicine, to support disease and trial awareness within institutions that are.
• Disease and Trial Awareness: Drive awareness of both the rare diseases being studied and the associated clinical trials and disease registries.
• Scientific Collaboration: Foster collaboration with HCPs and other stakeholders to support educational and data generation activities, ensuring alignment with scientific and organizational goals.
• Market Development: Engage and educate markets that may have limited familiarity with rare maternal-fetal diseases, including the introduction of new prenatal testing options, thus expanding the reach, and understanding of these areas.
• Scientific Insights: Collect valuable feedback and insights from the medical community to inform trial strategies and improve program outcomes.
• Non-Promotional Information Dissemination: Share accurate and relevant medical and scientific information in a non-promotional manner to support trial and disease awareness.

The MFI MSL plays a critical role in the success of the program by ensuring high scientific standards, fostering collaboration, and aligning with the organization's broader strategies.

Key Responsibilities

• Collaborate with the Director of MSLs to execute the overall program strategy, ensuring alignment with MSL/CTL organizational objectives.
• Boost recruitment into the Phase 3 trials
• Build and maintain trusted relationships with healthcare professionals, key opinion leaders (KOLs), clinical trial investigators/sites, and other stakeholders in assigned region.
• Gather and report scientific insights from the field to inform cross-functional teams and support organizational decision-making.
• The MSLs will support AZALEA, FREESIA, GERANIUM (the global HDFN registry), and PETUNIA (the MG pregnancy registry).
• Engaging in the exchange of scientific data and other medical and/or scientific information with external stakeholders
• Represent the organization at scientific meetings, conferences, and advisory boards as needed.
• Serve as a subject matter expert staying current with relevant scientific literature, clinical guidelines, and advancements.
• Support for strategic initiatives across Medical Affairs, Clinical Development, and other internal teams.
• Act as a liaison between internal teams and external stakeholders to support scientific exchange and collaboration.
• Operate with the highest ethical and professional standards, adhering to all applicable laws, regulations, and organizational policies.
• Ensure that all MSL and Clinical Trial activities are conducted in compliance with relevant guidelines and regulations.

Qualifications

• Advanced degree e.g., Ph.D, Pharm. D, MD, MSN, NP/PA or equivalent education required from